Prescription drug · UNAPPROVED DRUG OTHER
Phenobarbital NDC 16571-675
Phenobarbital 20 mg/5mL · Liquid · Oral · Rising Pharma Holdings, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 16571-675-16 | 16571067516 | 473 mL in 1 BOTTLE (16571-675-16)Marketed from Sep 1, 2020 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Phenobarbital
- Generic name (nonproprietary)
- phenobarbital
- Active ingredients
- Phenobarbital — 20 mg/5mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- Rising Pharma Holdings, Inc.NDC labeler code 16571
- Product type
- Prescription drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- DEA schedule
- CIV
- Identifiers
- Product ID 16571-675_a84eee2c-e36f-478c-8793-b153799ea38bSPL ID a84eee2c-e36f-478c-8793-b153799ea38bSPL set ID fe874f8a-4b56-4d2b-abf5-8742e2633a3bRxCUI 702519UNII YQE403BP4D
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N416571067516followed by a unit qualifier and the quantityPackage 16571-0675-16. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
INDICATIONS AND USAGE A. Sedative B. Anticonvulsant- For the treatment of generalized and partial seizures.
Excerpt only. Read the full label for complete information.
About NDC 16571-675
- What is NDC 16571-675?
- 16571-675 is the product NDC for Phenobarbital, Phenobarbital 20 mg/5mL liquid, listed with the FDA by Rising Pharma Holdings, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Phenobarbital.
- What is the active ingredient?
- Phenobarbital.
- Who is the labeler?
- Rising Pharma Holdings, Inc., NDC labeler code 16571. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Phenobarbital?
- 157 other product NDCs are listed under this name. See all Phenobarbital NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Phenobarbital products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Phenobarbital | Phenobarbital 15 mg/1 | TabletOral | Chartwell RX, LLC | 62135-510 | 62135-0510-90 |
| Phenobarbital | Phenobarbital 30 mg/1 | TabletOral | Chartwell RX, LLC | 62135-514 | 62135-0514-90 |
| Phenobarbital | Phenobarbital 60 mg/1 | TabletOral | Chartwell RX, LLC | 62135-515 | 62135-0515-90 |
| Phenobarbital | Phenobarbital 100 mg/1 | TabletOral | Chartwell RX, LLC | 62135-519 | 62135-0519-90 |
| Phenobarbital | Phenobarbital 16.2 mg/1 | TabletOral | Chartwell RX, LLC | 62135-539 | 62135-0539-90 |
| Phenobarbital | Phenobarbital 32.4 mg/1 | TabletOral | Chartwell RX, LLC | 62135-554 | 62135-0554-90 |
| Phenobarbital | Phenobarbital 97.2 mg/1 | TabletOral | Chartwell RX, LLC | 62135-558 | 62135-0558-90 |
| Phenobarbital | Phenobarbital 64.8 mg/1 | TabletOral | Chartwell RX, LLC | 62135-557 | 62135-0557-90 |
| Phenobarbital | Phenobarbital 16.2 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4719 | 70518-4719-00 |
| Phenobarbital | Phenobarbital 64.8 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4717 | 70518-4717-00 |